Seth Berger

Employment

• Tempus Labs (United States) Translational Genomics Director
  2026 - Present
• Ambry Genetics (United States) Translational Genomics Director
  2025 - Present
• Children's National Hospital Associate Professor

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (114)

• High Diagnosis Rate for Nonimmune Hydrops Fetalis With Prenatal Clinical Genome: Expanded Results From the Hydrops‐Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study
  American Journal of Medical Genetics Part A 2026 DOI: 10.1002/ajmg.a.70265
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• An extensible laboratory information management system for data harmonization across research centers: The ICTS Dashboard
  2026 DOI: 10.64898/2026.05.31.26354439
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• Sequencing approaches in hereditary cancer testing: strengths, limitations and future directions
  European Journal of Human Genetics 2026 DOI: 10.1038/s41431-026-02078-x
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• Kauro, a graph-based chatbot for high-fidelity information transmission conversations
  2026 DOI: 10.64898/2026.01.30.25342358
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• Response to Spurdle et al
  Genetics in Medicine 2026 DOI: 10.1016/j.gim.2025.101637
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• A Stepwise Approach to Macrocephaly: Clinical Clues to the Rare Diagnosis of PTEN Hamartoma Tumor Syndrome
  PEDIATRIC ANNALS 2026 DOI: 10.3928/19382359-20260309-02
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• Identification of de novo variants from parent-proband duos via long-read sequencing
  AMERICAN JOURNAL OF HUMAN GENETICS 2026 DOI: 10.1016/J.AJHG.2026.02.006
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• Large Class of Neurodevelopmental Disorders Requires Genome Sequencing for Diagnosis
  ANNALS OF NEUROLOGY 2026 DOI: 10.1002/ANA.78108
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• Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorder
  GENETICS IN MEDICINE 2026 DOI: 10.1016/J.GIM.2026.101685
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• GREGoR: accelerating genomics for rare diseases
  Nature 2025 DOI: 10.1038/s41586-025-09613-8
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